Acetone Cyanohydrin → HCID 178428877、化合物

A solution of 8.4 g (40 mmol) of 1,3-dicyclohexylcarbodiimide in 40 mL of acetonitrile was added to a mixture of 13.6 g (40 mmol) of 3-iodo-2-methyl-4-methylsulfonylbenzoic acid and 5.6 g (40 mmol) of 1-(1,1-dimethylethyl)-5-hydroxypyrazole in 80 mL of acetonitrile with stirring. The mixture was allowed to stir for 1 hour and was then filtered, washing the filter cake with a little acetonitrile. Triethylamine (16.8 mL, 120 mmol) and acetone cyanohydrin (1 mL, 10 mmol) were added with stirring to the filtrate. After about 1.5 hour, dichloromethane was added and the resulting mixture was washed with a mixture of 2N aqueous hydrochloric acid and saturated aqueous sodium chloride. It was then concentrated by evaporation under reduced pressure. The residue obtained was dissolved in dichloromethane and the resulting solution was extracted with dilute aqueous sodium hydroxide. The aqueous extract was acidified with concentrated aqueous hydrochloric acid and the resulting mixture was extracted with dichloromethane. Fifty mL of triethylamine was added to the dichloromethane extract and the resulting solution was washed with saturated aqueous sodium chloride solution and then several times with 2N aqueous hydrochloric acid. It was then concentrated by evaporation under reduced pressure. The residue was triturated with hexane to obtain 16.8 g (72.7 percent of theory of the title compound as a light yellow powder melting at 171-172° C.

1. stirringto stir for 1 hour
2. filtrationwas then filtered
3. washwashing the filter cake with a little acetonitrile
4. stirringwith stirring to the filtrate
5. washthe resulting mixture was washed with a mixture of 2N aqueous hydrochloric acid and saturated aqueous sodium chloride
6. concentrationIt was then concentrated by evaporation under reduced pressure
7. customThe residue obtained
8. extractionthe resulting solution was extracted with dilute aqueous sodium hydroxide
9. extractionThe aqueous extract
10. extractionthe resulting mixture was extracted with dichloromethane
11. additionFifty mL of triethylamine was added to the dichloromethane
12. extractionextract
13. washthe resulting solution was washed with saturated aqueous sodium chloride solution
14. concentrationIt was then concentrated by evaporation under reduced pressure
15. customThe residue was triturated with hexane

ORDレコード

ord-cc37f4b7a81140b3a7518d30c545d6fd

出典データセット

uspto-grants-2001_07

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US06265606B1